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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528658Generated: October 29, 2026

Trifluoroacetic acid → HCID 89761835, compound

https://huagongshe.com/reaction/528658

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 89761688HCID 89761688—
SolventDichloromethaneHCID 6344—
ProductHCID 89761835HCID 8976183520%

Reaction Steps

To a solution of 4-(2-(2-hydroxypropan-2-yl)phenyl)-N-(4-methoxybenzyl)-N-(thiazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonamide (300 mg, 0.543 mmol) in DCM (5 mL) was added TFA (0.4 mL, Spectrochem) at 0° C. The reaction mixture was stirred at ambient temperature for 2 h. After completion, the reaction mixture was quenched with saturated sodium bicarbonate solution (10 mL) and extracted with DCM (2×10 mL). The organic layer was dried over sodium sulfate and concentrated under reduced pressure to obtain crude material (47% by LCMS) that was purified by prep HPLC to obtain 4-(2-(prop-1-en-2-yl)phenyl)-N-(thiazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine-7-sulfonamide as a white solid (45 mg, 20.0%). MS (ESI, positive ion) m/z; 414.1 (M+1). 1H NMR (400 MHz, DMSO) δ 12.51 (s, 1H), 7.50-7.26 (m, 4H), 7.21 (d, J=4.6 Hz, 1H), 7.16-6.94 (m, 1H), 6.77 (d, J=4.5 Hz, 1H), 6.23 (d, J=8.4 Hz, 1H), 5.10 (s, 1H), 4.96 (s, 1H), 4.41-4.08 (m, 2H), 3.52 (d, J=11.7 Hz, 2H), 1.96 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346798B2
Source datasetuspto-grants-2016_05
ORD IDord-df8b97715efd4d16b4edab476da9a9c2
Source noteuspto-grants-2016_05